Molecular structure of 3-Acetylacetanilide, CAS Number: 7463-31-2
3-Acetylacetanilide (CAS 7463-31-2)
CAS Number:
7463-31-2
Molecular Weight:
177.20
Molecular Formula:
C10H11NO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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3-Acetylacetanilide (CAS 7463-31-2) References
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- Nitric oxide inhibits DNA synthesis and induces activation of poly(ADP-ribose) polymerase in cultured rat hepatocytes. | Dalmau, M., et al. 1996. Exp Cell Res. 228: 14-8. PMID: 8892965
- One‐Pot Synthesis of Unsymmetrical Benzils by Oxidative Coupling Using Selenium Dioxide and p‐Toluenesulfonic Acid Monohydrate. | Rohman, Md Rumum, et al. 2012. EurJOC. Volume 2012, Issue 2: 320-328.
- Acceptorless and base‐free dehydrogenation of alcohols and amines using ruthenium‐hydride complexes. | Muthaiah, Senthilkumar and Soon Hyeok Hong. 2012. Advanced Synthesis & Catalysis. 354.16: 3045-3053.
- Synthesis, Characterization and Antimicrobial Activity of Some Thiazole Derivatives. | SINGH, I. 2015. Chemical Science. 4.2: 458-462.
- Green Synthesis of New Pyrrolo [1, 2‐a] quinoxalines as Antiproliferative Agents in GPER‐expressing Breast Cancer Cells. | Carullo, Gabriele, et al. 2021. Journal of Chemistry. 2021.1: 5596816.
- Base‐Mediated N‐Acetylation of Anilines/Amines: Nitriles as a Surrogate of the Acetyl Group. | Kumar, Saurav, et al. 2023. ChemistrySelect. 8.1: e202204679.
- Capture of In Situ Generated Diazo Compounds or Copper Carbenoids by Triphenylphosphine: Selective Synthesis of trans‐Alkenes and Unsymmetric Azines via Reaction of Aldehydes with Ketone‐Derived N‐Tosylhydrazones. | Sha, Qiang, et al. 2145-2150. Advanced Synthesis & Catalysis. 355.11‐12: 2013.
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-Acetylacetanilide, 100 mg | sc-214118 | 100 mg | $300.00 |